# RGD-PIPELINE: ftp-file-extracts # MODULE: annotations-version-1.1.9 (Oct 10, 2019) # GENERATED-ON: 2025/02/01 # 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:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20241121 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:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20241121 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:0001486 abnormal startle reflex IEA N RGD:5509061 20241121 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:0001363 increased anxiety-related response IEA N RGD:5509061 20241121 MGI 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 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0013886 increased CD4-negative, CD25-positive NK T cell number IEA N RGD:5509061 20241121 MGI 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: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:0000609 abnormal liver physiology IAGP N RGD:5509061 20241219 MGI PMID:37216827 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:0003333 liver fibrosis IAGP N RGD:5509061 20241219 MGI PMID:37216827 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:0005165 increased susceptibility to injury IAGP N RGD:5509061 20241219 MGI PMID:37216827 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:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20241219 MGI PMID:37216827 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:0000689 abnormal spleen morphology IEA N RGD:5509061 20241121 MGI 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20241121 MGI 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 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0010099 abnormal thoracic cage shape IEA N RGD:5509061 20241121 MGI 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: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: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 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: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: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: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: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: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: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 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: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 10227 Bcan brevican gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20241121 MGI 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: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:0014587 impaired fine motor coordination IAGP N RGD:5509061 20241219 MGI PMID:17376154 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:0004924 abnormal behavior IEA N RGD:5509061 20241121 MGI 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 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20241121 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 10292 Cast calpastatin gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20241121 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 RG